Ensure compliance with cGMP, GLP, and regulatory guidelines. Maintain and review change controls, deviations, CAPA, and OOS/OOT records. Participate in internal audits, external audits, and regulatory inspections. Support data integrity. Review and support validation of equipment, process, cleaning, and analytical methods. Conduct trainings on GMP, SOPs, documentation practices, and quality systems.
Nothing to see here! Sessions in the future will show up here.